| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5164409 | Phytochemistry | 2015 | 9 Pages |
Abstract
A new type of glucosinolate hydrolysis product, a thiazolidine-2-one, was formed from a phenolic glucosinolate in one chemotype of Barbarea vulgaris. In both chemotypes, oxazolidine-2-thiones were also major products. The new glucosinolate product was formed in vitro with myrosinase and during autolysis.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Niels Agerbirk, Carl Erik Olsen,